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517-60-2

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517-60-2 Usage

Chemical Properties

Beige powder

Uses

Mellitic acid is part of a group of benzenepolycarboxylic acids that have potential anti-hemorrhagic properties. Mellitic acid is also used as a motif to investigate possible radial self-assembly using complementary aromatic bases.

Definition

ChEBI: A benzene-derived hexacarboxylic acid in which each carbon of benzene carries a carboxy substituent.

Check Digit Verification of cas no

The CAS Registry Mumber 517-60-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 517-60:
(5*5)+(4*1)+(3*7)+(2*6)+(1*0)=62
62 % 10 = 2
So 517-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H6O12/c13-7(14)1-2(8(15)16)4(10(19)20)6(12(23)24)5(11(21)22)3(1)9(17)18/h(H,13,14)(H,15,16)(H,17,18)(H,19,20)(H,21,22)(H,23,24)

517-60-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name mellitic acid

1.2 Other means of identification

Product number -
Other names Mellitic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:517-60-2 SDS

517-60-2Relevant articles and documents

-

Wibaut et al.

, p. 742,744, 745 (1941)

-

Schulz,Howard

, p. 991,993 (1946)

Ferris

, p. 387 (1964)

Access to aryl mellitic acid esters through a surprising oxidative esterification reaction

Geraskina, Margarita R.,Juetten, Mark J.,Winter, Arthur H.

, p. 5334 - 5337 (2014/06/23)

A serendipitously discovered oxidative esterification reaction of cyclohexane hexacarboxylic acid with phosphorus pentachloride and phenols provides one-pot access to previously unknown aryl mellitic acid esters. The reaction features a solvent-free digestion and chromatography-free purifications and demonstrates the possibility of cyclohexane-to-benzene conversions under relatively mild, metal-free conditions.

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